Steinert's disease, from assumption to certainty in neurological practice

Steinert’s disease, or myotonic dystrophy type 1 (MD1), is the most prevalent myopathy in adults. We report the case of a patient who was admitted to the Neurology Department for the progressive decrease in muscle strength in the lower limbs bilaterally. Symptoms began about 18 months before the pre...

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Main Authors: Vitalie Văcăraș, Hapca Elian, Ionuț-Dănuț Isachi, Cristiana Văcăraș, Dafin Fior Mureșanu
Format: Article
Language:English
Published: Romanian Association of Balneology, Editura Balneara 2022-09-01
Series:Balneo and PRM Research Journal
Subjects:
Online Access:http://bioclima.ro/Balneo515.pdf
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author Vitalie Văcăraș
Hapca Elian
Ionuț-Dănuț Isachi
Cristiana Văcăraș
Dafin Fior Mureșanu
author_facet Vitalie Văcăraș
Hapca Elian
Ionuț-Dănuț Isachi
Cristiana Văcăraș
Dafin Fior Mureșanu
author_sort Vitalie Văcăraș
collection DOAJ
description Steinert’s disease, or myotonic dystrophy type 1 (MD1), is the most prevalent myopathy in adults. We report the case of a patient who was admitted to the Neurology Department for the progressive decrease in muscle strength in the lower limbs bilaterally. Symptoms began about 18 months before the presentation to the Neurology Department. On the elec-troneurographic examination, specific features for myotonic dystrophy type 1 were described, confirmed later by the genetic test.
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spelling doaj.art-7f30755c0297425888035ede44daba9e2022-12-22T03:48:25ZengRomanian Association of Balneology, Editura BalnearaBalneo and PRM Research Journal2734-84582022-09-0113351510.12680/balneo.2022.515Steinert's disease, from assumption to certainty in neurological practiceVitalie VăcărașHapca ElianIonuț-Dănuț IsachiCristiana VăcărașDafin Fior MureșanuSteinert’s disease, or myotonic dystrophy type 1 (MD1), is the most prevalent myopathy in adults. We report the case of a patient who was admitted to the Neurology Department for the progressive decrease in muscle strength in the lower limbs bilaterally. Symptoms began about 18 months before the presentation to the Neurology Department. On the elec-troneurographic examination, specific features for myotonic dystrophy type 1 were described, confirmed later by the genetic test. http://bioclima.ro/Balneo515.pdfsteinert’s diseaseparaparesismultisystemic diseaseneurology
spellingShingle Vitalie Văcăraș
Hapca Elian
Ionuț-Dănuț Isachi
Cristiana Văcăraș
Dafin Fior Mureșanu
Steinert's disease, from assumption to certainty in neurological practice
Balneo and PRM Research Journal
steinert’s disease
paraparesis
multisystemic disease
neurology
title Steinert's disease, from assumption to certainty in neurological practice
title_full Steinert's disease, from assumption to certainty in neurological practice
title_fullStr Steinert's disease, from assumption to certainty in neurological practice
title_full_unstemmed Steinert's disease, from assumption to certainty in neurological practice
title_short Steinert's disease, from assumption to certainty in neurological practice
title_sort steinert s disease from assumption to certainty in neurological practice
topic steinert’s disease
paraparesis
multisystemic disease
neurology
url http://bioclima.ro/Balneo515.pdf
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AT cristianavacaras steinertsdiseasefromassumptiontocertaintyinneurologicalpractice
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